Zenara, a Biophore Company, has announced a Walk-In Interview Drive for experienced professionals in the Quality Control and Production Track & Trace departments. Candidates with experience in pharmaceutical formulation manufacturing are invited to attend the interview. Immediate joiners with relevant technical expertise are preferred.

Job Overview

Particular Details

Company Name

Zenara (A Biophore Company)

Job Type

Walk-In Interview

Interview Dates

03 August 2026 to 07 August 2026

Interview Time

10:00 AM to 3:00 PM

Industry

Pharmaceutical – Formulation

Preferred Candidates

Immediate Joiners

Available Positions

1. Quality Control (QC)

Position

Executive

Junior Executive – HPLC & Wet Analysis

Qualification

B.Pharm

M.Pharm

Experience

3 to 5 Years

Required Technical Skills

Hands-on knowledge of HPLC Method Validation (MV)

Experience in Wet Analysis

Strong understanding of Chromatographic Techniques

Knowledge of cGLP compliance

Familiarity with 21 CFR Part 11 requirements

2. Production – Track & Trace

Position

Executive

Junior Executive

Qualification

ITI

Diploma

B.Tech

Experience

3 to 5 Years

Required Technical Skills

Master data entry and template creation

Product registration in Track & Trace systems

Coordination with serialization vendors

Troubleshooting serialization-related issues

Execution and verification of label reconciliation

Understanding of pharmaceutical serialization processes

Documents Required

Candidates should carry the following documents:

Updated Resume

Last 3 Months’ Payslips

Current CTC Details

Educational Certificates (Photocopies)

Aadhaar Card Copy

PAN Card Copy

Important Notes

Only candidates from Formulation background will be considered.

Immediate joiners are preferred.

The company has clearly stated that it is not associated with any manpower consultancy.

Candidates should attend the interview only if they meet the eligibility criteria.

Why Join Zenara?

Zenara, a Biophore Company, offers an opportunity to work in a regulated pharmaceutical manufacturing environment with exposure to advanced analytical techniques, serialization systems, regulatory compliance, and quality-focused manufacturing practices.

Technical FAQs

1. What is HPLC Method Validation in pharmaceutical quality control?

HPLC Method Validation is the process of proving that an analytical method consistently produces accurate, precise, specific, and reliable results according to ICH guidelines.

2. What is Wet Analysis?

Wet Analysis involves laboratory testing using chemical reagents for identification, assay, impurity analysis, and quality evaluation of pharmaceutical materials.

3. What is 21 CFR Part 11?

21 CFR Part 11 is a US FDA regulation governing electronic records and electronic signatures to ensure data integrity, security, and traceability in pharmaceutical companies.

4. What is Track & Trace in pharmaceutical manufacturing?

Track & Trace is a serialization system that assigns unique identification codes to medicine packs, helping prevent counterfeit products and ensuring supply chain visibility.

5. What is Label Reconciliation?

Label reconciliation is the verification process of issued, used, damaged, and unused labels during packaging to ensure accountability and prevent mix-ups.